2,4-Bis(trifluoromethyl)benzyl alcohol

2,4-Bis(trifluoromethyl)benzyl alcohol Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Alfa Aesar  
Tel: 400-6106006
Email: saleschina@alfa-asia.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
2,4-Bis(trifluoromethyl)benzyl alcohol Basic information
Product Name:2,4-Bis(trifluoromethyl)benzyl alcohol
Synonyms:RARECHEM AL BD 0344;2,4-Bis(trifluoromethyl)benzyl alcohol 98%;2,4-Bis(trifluoromethyl)benzylalcohol98%;2,4-DI(TRIFLUOROMETHYL)BENZYL ALCOHOL;Benzenemethanol, 2,4-bis(trifluoromethyl)-;2,4-bis(trifluoromethyl)benzenemethylol;(2,4-BIS(TRIFLUOROMETHYL)PHENYL)METHANOL;2,4-Bis(trifluoromethyl)benzyl alcohol
CAS:143158-15-0
MF:C9H6F6O
MW:244.13
EINECS:
Product Categories:
Mol File:143158-15-0.mol
2,4-Bis(trifluoromethyl)benzyl alcohol Structure
2,4-Bis(trifluoromethyl)benzyl alcohol Chemical Properties
Boiling point 181.3±35.0 °C(Predicted)
density 1.433±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka13.59±0.10(Predicted)
AppearanceWhite to off-white Solid
CAS DataBase Reference143158-15-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36-22
Safety Statements 26-36
HazardClass IRRITANT
HS Code 2906290090
MSDS Information
ProviderLanguage
ALFA English
2,4-Bis(trifluoromethyl)benzyl alcohol Usage And Synthesis
Synthesis
2,4-BIS(TRIFLUOROMETHYL)BENZALDEHYDE

59664-42-5

2,4-BIS(TRIFLUOROMETHYL)BENZYL ALCOHOL

143158-15-0

GENERAL METHOD: Sodium borohydride (0.28 g, 7.5 mmol) was added batchwise to a methanol (10 mL) solution of 2,4-bis(trifluoromethyl)benzaldehyde (5 mmol) cooled in an ice bath over a period of 20 minutes. The reaction mixture was stirred at room temperature for 30 min. Excess sodium borohydride was quenched by addition of ice. Subsequently, the reaction mixture was concentrated and the residue was dissolved in ethyl acetate and washed twice with deionized water. The organic phase was dried with anhydrous sodium sulfate and concentrated to give 2,4-bis(trifluoromethyl)benzyl alcohol in 96% yield as a colorless oil. The spectral data of the resulting compound were in agreement with standard samples from commercial sources.

References[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 2, p. 721 - 737
2,4-Bis(trifluoromethyl)benzyl alcohol Preparation Products And Raw materials
Raw materials2,4-Bis(trifluoromethyl)benzaldehyde-->Sodium borohydride-->Methanol
Tag:2,4-Bis(trifluoromethyl)benzyl alcohol(143158-15-0) Related Product Information
2,5-Bis(trifluoromethyl)benzyl alcohol 2,4-Bis(trifluoromethyl)benzyl alcohol 4-(Hexafluoro-2-hydroxyisopropyl)aniline 3,5-BIS(TRIFLUOROMETHYL)BENZYL ALCOHOL,3,5-Bis(trifluoromethyl)benzyl alcohol 98% à-Methyl-3,5-bis-(trifluoromethyl)-benzyl alcohol,alpha-Methyl-3,5-bis(trifluoromethyl)benzyl alcohol α,α-bis(trifluoromethyl)benzyl alcohol,à,à-bis(trifluoromethyl)benzyl alcohol,ALPHA,ALPHA-BIS(TRIFLUOROMETHYL)BENZYL ALCOHOL 4-methyl-alpha,alpha-bis(trifluoromethyl)benzyl alcohol 2,4-BIS(TRIFLUOROMETHYL)BENZOIC ACID 2,4,6-TRIS(TRIFLUOROMETHYL)BENZOIC ACID 2-Fluoro-4,6-bis(trifluoromethyl)benzoic acid 2-Methoxy-4,6-di(trifluoromethyl)benzoic acid 2-Fluoro-4,6-bis(trifluoromethyl)benzyl alcohol 1,1,1,3,3,3-Hexafluoro-2-(4-hydroxyphenyl)propan-2-ol 3-[4-(2,4-Bis-trifluoromethylbenzyloxy)-3-methoxyphenyl]-2-cyano-N-(5-trifluoromethyl-1,3,4-thiadiazol-2-yl)acrylamide 2,4-Bis(trifluoromethyl)-6-chlorobenzoic acid RARECHEM AL BF 0344 RARECHEM AL BP 0344 RARECHEM AL BI 0344